file1
,
file2
, etc. all in the same folder or directory;
first, locate one of the files with the [Browse...] button. Then alter the
file path in the box above to include '*' character (eg. file*
).
Wildcard '?' to blanket only one character works too.Historiographs |
Grand Totals: LCS 404, GCS 46055, CR 26988, NA 5433 Collection span: 1991 - 2007 (17 years) | |
Title Word List (2075) Word count: 4279, All words count: 6226 |
# | Word | Recs | Percent | TLCS | TGCS |
---|---|---|---|---|---|
1401 | LAB | 1 | 0.2 | 3 | 62 |
1402 | LADDERS | 1 | 0.2 | 0 | 77 |
1403 | LANGUAGE | 1 | 0.2 | 0 | 242 |
1404 | LATERAL | 1 | 0.2 | 1 | 81 |
1405 | LATEX | 1 | 0.2 | 0 | 79 |
1406 | LATTICE | 1 | 0.2 | 0 | 84 |
1407 | LAW | 1 | 0.2 | 0 | 53 |
1408 | LEGACY | 1 | 0.2 | 0 | 280 |
1409 | LENGTH | 1 | 0.2 | 0 | 129 |
1410 | LENNARD | 1 | 0.2 | 0 | 111 |
1411 | LEVEL | 1 | 0.2 | 0 | 59 |
1412 | LEVETIRACETAM | 1 | 0.2 | 0 | 97 |
1413 | LIE | 1 | 0.2 | 0 | 73 |
1414 | LIFETIME | 1 | 0.2 | 1 | 53 |
1415 | LINEAR | 1 | 0.2 | 0 | 66 |
1416 | LINKED | 1 | 0.2 | 0 | 54 |
1417 | LINKER | 1 | 0.2 | 3 | 144 |
1418 | LIPOFUSCIN | 1 | 0.2 | 0 | 96 |
1419 | LIPOPHILICITY | 1 | 0.2 | 1 | 67 |
1420 | LIPOXYGENASES | 1 | 0.2 | 0 | 137 |
1421 | LIQUIDS | 1 | 0.2 | 0 | 64 |
1422 | LNCAP | 1 | 0.2 | 0 | 59 |
1423 | LOAD | 1 | 0.2 | 0 | 71 |
1424 | LOADED | 1 | 0.2 | 0 | 58 |
1425 | LOCALISATION | 1 | 0.2 | 0 | 72 |
1426 | LOCATION | 1 | 0.2 | 1 | 58 |
1427 | LOCKED | 1 | 0.2 | 0 | 73 |
1428 | LOGIC | 1 | 0.2 | 0 | 106 |
1429 | LOGISTIC | 1 | 0.2 | 0 | 85 |
1430 | LOSS | 1 | 0.2 | 0 | 65 |
# | Word | Recs | Percent | TLCS | TGCS |
1431 | LTP | 1 | 0.2 | 0 | 129 |
1432 | LUALO3 | 1 | 0.2 | 0 | 56 |
1433 | LUBRICANTS | 1 | 0.2 | 0 | 54 |
1434 | LUMEN | 1 | 0.2 | 0 | 82 |
1435 | LUMINESCENCE | 1 | 0.2 | 0 | 76 |
1436 | MACROCYCLIC | 1 | 0.2 | 0 | 56 |
1437 | MACRODROPLETS | 1 | 0.2 | 1 | 62 |
1438 | MACROSCOPIC | 1 | 0.2 | 0 | 55 |
1439 | MAGELLANIC | 1 | 0.2 | 1 | 58 |
1440 | MAGMATISM | 1 | 0.2 | 0 | 53 |
1441 | MAGNETISM | 1 | 0.2 | 0 | 53 |
1442 | MAGNETO | 1 | 0.2 | 0 | 123 |
1443 | MAGNETOGRAMS | 1 | 0.2 | 1 | 72 |
1444 | MAGNETORESISTANCE | 1 | 0.2 | 0 | 53 |
1445 | MAGNETOSTATIC | 1 | 0.2 | 0 | 53 |
1446 | MAGNETOSTRAIN | 1 | 0.2 | 1 | 63 |
1447 | MAGNETOTHERMAL | 1 | 0.2 | 0 | 80 |
1448 | MAGNON | 1 | 0.2 | 1 | 54 |
1449 | MAIN | 1 | 0.2 | 3 | 99 |
1450 | MAJOR | 1 | 0.2 | 0 | 56 |
1451 | MANIFESTATIONS | 1 | 0.2 | 0 | 56 |
1452 | MAPS | 1 | 0.2 | 0 | 85 |
1453 | MARINE | 1 | 0.2 | 0 | 56 |
1454 | MARTENSITE | 1 | 0.2 | 0 | 55 |
1455 | MASSIVE | 1 | 0.2 | 0 | 130 |
1456 | MATERIALS | 1 | 0.2 | 0 | 90 |
1457 | MATRICES | 1 | 0.2 | 3 | 66 |
1458 | MEASURED | 1 | 0.2 | 1 | 84 |
1459 | MECHANISMS | 1 | 0.2 | 0 | 96 |
1460 | MECHANISTIC | 1 | 0.2 | 0 | 62 |
# | Word | Recs | Percent | TLCS | TGCS |
1461 | MEDICINAL | 1 | 0.2 | 0 | 194 |
1462 | MEDIUM | 1 | 0.2 | 1 | 60 |
1463 | MELTING | 1 | 0.2 | 0 | 84 |
1464 | MELTS | 1 | 0.2 | 1 | 167 |
1465 | MEMANTINE | 1 | 0.2 | 0 | 61 |
1466 | MEMBERED | 1 | 0.2 | 0 | 56 |
1467 | MESONS | 1 | 0.2 | 1 | 58 |
1468 | METALS | 1 | 0.2 | 0 | 82 |
1469 | METAMORPHIC | 1 | 0.2 | 0 | 131 |
1470 | METASTABLE | 1 | 0.2 | 0 | 71 |
1471 | METASTASES | 1 | 0.2 | 0 | 67 |
1472 | METASTASIS | 1 | 0.2 | 0 | 137 |
1473 | METHANE | 1 | 0.2 | 0 | 179 |
1474 | METHODS | 1 | 0.2 | 0 | 61 |
1475 | MG2 | 1 | 0.2 | 4 | 66 |
1476 | MICE | 1 | 0.2 | 1 | 117 |
1477 | MICRO | 1 | 0.2 | 0 | 65 |
1478 | MICROBIAL | 1 | 0.2 | 0 | 179 |
1479 | MICROCOCCUS | 1 | 0.2 | 0 | 130 |
1480 | MICRODOMAINS | 1 | 0.2 | 0 | 109 |
1481 | MICROHYDRATED | 1 | 0.2 | 0 | 72 |
1482 | MICROINDENTATIONS | 1 | 0.2 | 0 | 262 |
1483 | MICROMETRE | 1 | 0.2 | 0 | 201 |
1484 | MICRON | 1 | 0.2 | 2 | 86 |
1485 | MICROSPECTROSCOPY | 1 | 0.2 | 0 | 79 |
1486 | MID | 1 | 0.2 | 1 | 75 |
1487 | MINERAL | 1 | 0.2 | 0 | 73 |
1488 | MINIPROBE | 1 | 0.2 | 4 | 71 |
1489 | MITOCHONDRIA | 1 | 0.2 | 0 | 84 |
1490 | MITOTIC | 1 | 0.2 | 0 | 67 |
# | Word | Recs | Percent | TLCS | TGCS |
1491 | MIXED | 1 | 0.2 | 1 | 136 |
1492 | MIXING | 1 | 0.2 | 0 | 89 |
1493 | MOBILIZATION | 1 | 0.2 | 0 | 67 |
1494 | MODAL | 1 | 0.2 | 0 | 59 |
1495 | MODELLING | 1 | 0.2 | 0 | 131 |
1496 | MODERN | 1 | 0.2 | 0 | 195 |
1497 | MODIFIED | 1 | 0.2 | 0 | 74 |
1498 | MODULATES | 1 | 0.2 | 2 | 65 |
1499 | MODULATORS | 1 | 0.2 | 0 | 129 |
1500 | MOLA | 1 | 0.2 | 1 | 68 |
1501 | MOLAR | 1 | 0.2 | 0 | 56 |
1502 | MOLECULE | 1 | 0.2 | 0 | 53 |
1503 | MONASTROL | 1 | 0.2 | 0 | 67 |
1504 | MONITORING | 1 | 0.2 | 0 | 55 |
1505 | MONO | 1 | 0.2 | 0 | 143 |
1506 | MONODISPERSE | 1 | 0.2 | 0 | 67 |
1507 | MONODOMAIN | 1 | 0.2 | 1 | 53 |
1508 | MONOHYDRATED | 1 | 0.2 | 0 | 52 |
1509 | MONOMER | 1 | 0.2 | 0 | 71 |
1510 | MONSOONAL | 1 | 0.2 | 0 | 52 |
1511 | MOON | 1 | 0.2 | 0 | 81 |
1512 | MORTALITY | 1 | 0.2 | 0 | 175 |
1513 | MOTION | 1 | 0.2 | 0 | 123 |
1514 | MOTORS | 1 | 0.2 | 0 | 76 |
1515 | MOUSE | 1 | 0.2 | 2 | 53 |
1516 | MP2 | 1 | 0.2 | 0 | 52 |
1517 | MPC | 1 | 0.2 | 3 | 57 |
1518 | MULTIDIMENSIONAL | 1 | 0.2 | 0 | 59 |
1519 | MULTIELEMENT | 1 | 0.2 | 4 | 71 |
1520 | MULTIPARAMETRIC | 1 | 0.2 | 0 | 72 |
# | Word | Recs | Percent | TLCS | TGCS |
1521 | MULTIPLICITIES | 1 | 0.2 | 2 | 86 |
1522 | MULTIWAVELENGTH | 1 | 0.2 | 2 | 101 |
1523 | MURINE | 1 | 0.2 | 0 | 106 |
1524 | MUTAGENESIS | 1 | 0.2 | 0 | 86 |
1525 | MYOCARDIAL | 1 | 0.2 | 0 | 60 |
1526 | NABARRO | 1 | 0.2 | 0 | 128 |
1527 | NAMES | 1 | 0.2 | 0 | 59 |
1528 | NANC | 1 | 0.2 | 0 | 56 |
1529 | NANOTRIBOLOGICAL | 1 | 0.2 | 0 | 54 |
1530 | NANOTUBE | 1 | 0.2 | 0 | 93 |
1531 | NAPHTHOL | 1 | 0.2 | 0 | 58 |
1532 | NCAM | 1 | 0.2 | 0 | 345 |
1533 | NEBIVOLOL | 1 | 0.2 | 0 | 175 |
1534 | NEIGHBORING | 1 | 0.2 | 0 | 124 |
1535 | NEIGHBOURHOOD | 1 | 0.2 | 0 | 67 |
1536 | NEMATODA | 1 | 0.2 | 0 | 59 |
1537 | NEOCLASSICAL | 1 | 0.2 | 0 | 58 |
1538 | NEOPLASMS | 1 | 0.2 | 2 | 66 |
1539 | NESDIS | 1 | 0.2 | 0 | 65 |
1540 | NESTERENKONIA | 1 | 0.2 | 0 | 130 |
1541 | NESTIN | 1 | 0.2 | 0 | 106 |
1542 | NEURON | 1 | 0.2 | 0 | 53 |
1543 | NEURONES | 1 | 0.2 | 1 | 154 |
1544 | NEUTRINO | 1 | 0.2 | 3 | 96 |
1545 | NEWLY | 1 | 0.2 | 0 | 74 |
1546 | NIMNGA | 1 | 0.2 | 1 | 107 |
1547 | NMDA | 1 | 0.2 | 0 | 61 |
1548 | NOAA | 1 | 0.2 | 0 | 65 |
1549 | NOMENCLATURE | 1 | 0.2 | 0 | 261 |
1550 | NONCODING | 1 | 0.2 | 1 | 65 |
# | Word | Recs | Percent | TLCS | TGCS |
1551 | NONCOVALENTLY | 1 | 0.2 | 4 | 90 |
1552 | NONEQUILIBRIUM | 1 | 0.2 | 3 | 82 |
1553 | NONIONIZED | 1 | 0.2 | 0 | 52 |
1554 | NONLINEARITY | 1 | 0.2 | 1 | 130 |
1555 | NONUNIFORM | 1 | 0.2 | 1 | 60 |
1556 | NORTH | 1 | 0.2 | 0 | 65 |
1557 | NORTHERN | 1 | 0.2 | 0 | 78 |
1558 | NOV | 1 | 0.2 | 0 | 130 |
1559 | NUCLEIC | 1 | 0.2 | 0 | 72 |
1560 | NUCLEUS | 1 | 0.2 | 2 | 165 |
1561 | NULL | 1 | 0.2 | 1 | 54 |
1562 | NUMBER | 1 | 0.2 | 3 | 68 |
1563 | OBSERVATION | 1 | 0.2 | 1 | 89 |
1564 | OBSERVED | 1 | 0.2 | 1 | 51 |
1565 | OBTAINED | 1 | 0.2 | 0 | 74 |
1566 | OCCURRING | 1 | 0.2 | 0 | 195 |
1567 | OCEANS | 1 | 0.2 | 0 | 114 |
1568 | OCTAHYDROXY | 1 | 0.2 | 0 | 63 |
1569 | OCTANOL | 1 | 0.2 | 3 | 88 |
1570 | OCULAR | 1 | 0.2 | 0 | 63 |
1571 | OLIGODENDROCYTES | 1 | 0.2 | 1 | 78 |
1572 | OLIGOFLUORENE | 1 | 0.2 | 0 | 67 |
1573 | OMAN | 1 | 0.2 | 0 | 131 |
1574 | OMBROTROPHIC | 1 | 0.2 | 0 | 92 |
1575 | OMEGA | 1 | 0.2 | 0 | 86 |
1576 | ONE | 1 | 0.2 | 2 | 217 |
1577 | OPERATED | 1 | 0.2 | 0 | 59 |
1578 | OPERATORS | 1 | 0.2 | 0 | 52 |
1579 | OPPOSITE | 1 | 0.2 | 4 | 90 |
1580 | OPPOSITION | 1 | 0.2 | 0 | 51 |
# | Word | Recs | Percent | TLCS | TGCS |
1581 | OPTIMIZED | 1 | 0.2 | 0 | 73 |
1582 | ORAL | 1 | 0.2 | 0 | 63 |
1583 | ORBITALS | 1 | 0.2 | 0 | 52 |
1584 | ORBITER | 1 | 0.2 | 0 | 114 |
1585 | ORDERED | 1 | 0.2 | 0 | 62 |
1586 | ORGANELLES | 1 | 0.2 | 0 | 53 |
1587 | ORGANOPHOSPHORUS | 1 | 0.2 | 0 | 117 |
1588 | ORIENTED | 1 | 0.2 | 0 | 262 |
1589 | OUTBURST | 1 | 0.2 | 0 | 72 |
1590 | OUTER | 1 | 0.2 | 0 | 84 |
1591 | OUTPUT | 1 | 0.2 | 0 | 76 |
1592 | OVERFITTING | 1 | 0.2 | 5 | 103 |
1593 | OVERTONE | 1 | 0.2 | 0 | 79 |
1594 | OVERTRAINING | 1 | 0.2 | 5 | 103 |
1595 | OXIDATIVE | 1 | 0.2 | 0 | 93 |
1596 | OXIDES | 1 | 0.2 | 0 | 66 |
1597 | OXIDIZED | 1 | 0.2 | 0 | 70 |
1598 | OXYTOCIN | 1 | 0.2 | 1 | 53 |
1599 | P2X | 1 | 0.2 | 0 | 103 |
1600 | P70 | 1 | 0.2 | 0 | 66 |